- Oura (New York, NY)
- …are compliant with the applicable standards and regulations governing the development of medical device software at Oura. This role will demand close ... assessments, testing, etc. by applying applicable company procedures and regulatory requirements. + Perform a broad variety of tasks...of experience working in a regulated environment under a medical device Quality Management System (21 CFR… more
- Rush University Medical Center (Chicago, IL)
- …including contacting Bone and Tissue Bank representatives for allografts and medical device representatives for prostheses and instruments. * Comprehensively ... **Job Description** Location: Chicago, Illinois Business Unit: Rush Medical Group Hospital: Rush University Medical ...candidates will also meet all other state and federal regulatory practice and accreditation standards. Rush has over 400… more
- Veterans Affairs, Veterans Health Administration (Philadelphia, PA)
- …This is above the full performance level for the Supervisory Medical Instrument Technician (Vascular) requiring specialized advanced knowledge and assignments. The ... work involves operating or monitoring diagnostic and therapeutic medical instruments and equipment associated with vascular and general sonography duties, to include… more
- Veterans Affairs, Veterans Health Administration (Pittsburgh, PA)
- …of the medical physics quality assurance program. The CTMP ensures regulatory compliance with the healthcare system's radiation safety program and works closely ... This position is located within the Oncology department at the Pittsburgh VA Medical Center, in Pittsburgh, PA. The Therapeutic Medical Physicist(Advance Level)… more
- Terumo Neuro (Aliso Viejo, CA)
- …and experience. 2. Minimum five (5) years of relevant experience in product labeling in medical device field. 3. Minimum one (1) year of experience in project ... 12. Minimum seven (7) years of relevant experience in product labeling in medical device field. **External-Facing Title:** Sr Labeling Lead **Posting Country:**… more
- Actalent (Minneapolis, MN)
- …improvement activities as assigned. + Monitor the company's drug or medical devices surveillance program, including intake, protocol development, evaluation, ... is provided and conduct follow-up as needed. + Determine regulatory reporting status and complete regulatory reports...+ Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience… more
- Abbott (Burlington, MA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... of education and work experience + Minimum 5 years leading projects in a medical device , biomedical or high technology industry. + Strong communication skills,… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- …supervision facilitating and tracking the approval of labeling artwork for finished medical devices . This position includes the below responsibilities, as well ... scanning activities and documentation. + Supports the labeling work stream for revisions to medical device product labeling. + Track and monitor the approval and… more
- J&J Family of Companies (Irvine, CA)
- …+ Minimum of 6 years of relevant experience in clinical research within Medical Device or Pharmaceuticals, with demonstrated expertise in statistical design, ... rigor, regulatory compliance, and strategic alignment in support of device evidence generation. + Independently develop statistical analysis plans for diverse… more
- J&J Family of Companies (Cincinnati, OH)
- …lead the development and execution of toxicology and biocompatibility evaluations for surgical medical device products. This role will be pivotal in expanding ... of experience in toxicology/biocompatibility, with a strong focus in the pharmaceutical or medical device industries. + Board Certification in ATS, DABT, or… more